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- W2951606377 abstract "Abstract gem-Borazirconocenes, 1 , readily add across Michael acceptors in the presence of Cu(I)Br·SMe2, to afford 1,4-addition products in good to excellent yields. In the case of cycloalkenones diastereomers are produced, with the anti product favored. The selectivity with cyclopentenone is high (9:1), while with cyclohexenone it is less (3:1). In the present content, gem-borazirconocene alkanes can be regarded as α-hydroxyl anion equivalents." @default.
- W2951606377 created "2019-06-27" @default.
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- W2951606377 date "2010-08-17" @default.
- W2951606377 modified "2023-09-25" @default.
- W2951606377 title "ChemInform Abstract: Conjugate Addition of gem-Borazirconocene Alkanes to Michael Acceptors." @default.
- W2951606377 cites W2084309153 @default.
- W2951606377 doi "https://doi.org/10.1002/chin.199529223" @default.
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